HDAC6 is a microtubule-associated deacetylase

• Published in: Nature (London) 2002-05, Vol.417 (6887), p.455-458
• Main Authors: Yao, Tso-Pang, Hubbert, Charlotte, Guardiola, Amaris, Shao, Rong, Kawaguchi, Yoshiharu, Ito, Akihiro, Nixon, Andrew, Yoshida, Minoru, Wang, Xiao-Fan
• Format: Article
• Language: English
• Subjects: 3T3 Cells; Acetylation; Animals; Biological and medical sciences; Cell structures and functions; Cellular biology; Chemotaxis; Cytoskeleton, cytoplasm. Intracellular movements; Enzymes; Fundamental and applied biological sciences. Psychology; HDAC6 protein; Histone Deacetylase 6; Histone Deacetylases - genetics; Histone Deacetylases - metabolism; Mice; Microtubule-Associated Proteins - genetics; Microtubule-Associated Proteins - metabolism; Microtubules - chemistry; Microtubules - metabolism; Molecular and cellular biology; Protein Binding; Proteins; Tubulin - chemistry; Tubulin - metabolism; tubulin deacetylase
• ISSN: 0028-0836; 1476-4687
• DOI: 10.1038/417455a

Reversible acetylation of α-tubulin has been implicated in regulating microtubule stability and function. The distribution of acetylated α-tubulin is tightly controlled and stereotypic. Acetylated α-tubulin is most abundant in stable microtubules but is absent from dynamic cellular structures such as neuronal growth cones and the leading edges of fibroblasts. However, the enzymes responsible for regulating tubulin acetylation and deacetylation are not known. Here we report that a member of the histone deacetylase family, HDAC6, functions as a tubulin deacetylase. HDAC6 is localized exclusively in the cytoplasm, where it associates with microtubules and localizes with the microtubule motor complex containing p150glued (ref. 3). In vivo, the overexpression of HDAC6 leads to a global deacetylation of α-tubulin, whereas a decrease in HDAC6 increases α-tubulin acetylation. In vitro, purified HDAC6 potently deacetylates α-tubulin in assembled microtubules. Furthermore, overexpression of HDAC6 promotes chemotactic cell movement, supporting the idea that HDAC6-mediated deacetylation regulates microtubule-dependent cell motility. Our results show that HDAC6 is the tubulin deacetylase, and provide evidence that reversible acetylation regulates important biological processes beyond histone metabolism and gene transcription.